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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1976 - 2000 of 5716 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0081226
  • autosomal recessive intellectual developmental disorder 65
Homo sapiens (human)
DOID:0081228
  • autosomal recessive intellectual developmental disorder 67
Homo sapiens (human)
DOID:0081230
  • autosomal recessive intellectual developmental disorder 69
Homo sapiens (human)
DOID:0081231
  • autosomal recessive intellectual developmental disorder 70
Homo sapiens (human)
DOID:0081234
  • autosomal recessive intellectual developmental disorder 75
Homo sapiens (human)
DOID:0081235
  • autosomal recessive intellectual developmental disorder 76
Homo sapiens (human)
DOID:0081236
  • autosomal recessive intellectual developmental disorder 77
Homo sapiens (human)
DOID:0081237
  • acromesomelic dysplasia 3
  • Aliases:
    • Demirhan-type acromesomelic dysplasia
Homo sapiens (human)
DOID:0081242
  • autoimmune interstitial lung, joint, and kidney disease
  • Aliases:
    • Autoimmune interstitial lung disease-arthritis syndrome
    • COPA syndrome
Mus musculus (house mouse)
DOID:0081242
  • autoimmune interstitial lung, joint, and kidney disease
  • Aliases:
    • Autoimmune interstitial lung disease-arthritis syndrome
    • COPA syndrome
Homo sapiens (human)
DOID:0081243
  • rhizomelic chondrodysplasia punctate type 4
Homo sapiens (human)
DOID:0081263
  • neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
  • Aliases:
    • NEDMCR syndrome
Homo sapiens (human)
DOID:0081265
  • intellectual developmental disorder with abnormal behavior, microcephaly, and short stature
  • Aliases:
    • IDDBAS
Homo sapiens (human)
DOID:0081266
  • pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
  • Aliases:
    • PAMDDFS
Homo sapiens (human)
DOID:0081267
  • graft-versus-host disease
  • Aliases:
    • GvHD
    • graft versus host disease
Homo sapiens (human)
DOID:0081268
  • pulmonary venoocclusive disease 1
Homo sapiens (human)
DOID:0081270
  • Smith-McCort dysplasia 1
Homo sapiens (human)
DOID:0081271
  • Smith-McCort dysplasia 2
Homo sapiens (human)
DOID:0081272
  • Sandestig-Stefanova syndrome
Homo sapiens (human)
DOID:0081274
  • peroxisome biogenesis disorder 14B
Homo sapiens (human)
DOID:0081276
  • cerebellar atrophy, visual impairment, and psychomotor retardation
  • Aliases:
    • CAVIPMR
Homo sapiens (human)
DOID:0081288
  • white sponge nevus 2
Homo sapiens (human)
DOID:0081289
  • Antley-Bixler syndrome
  • Aliases:
    • Antley Bixler syndrome
    • Antley and Bixler's syndrome
Homo sapiens (human)
DOID:0081290
  • Antley-Bixler syndrome without disordered steroidogenesis
Homo sapiens (human)
DOID:0081292
  • traumatic brain injury
Homo sapiens (human)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 6, 2026